rs794727123

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs794727123(A;A)

Make rs794727123(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

32573744

Gene

DMD

is a	snp
is	mentioned by
dbSNP	rs794727123
dbSNP (classic)	rs794727123
ClinGen	rs794727123
ebi	rs794727123
HLI	rs794727123
Exac	rs794727123
Gnomad	rs794727123
Varsome	rs794727123
LitVar	rs794727123
Map	rs794727123
PheGenI	rs794727123
Biobank	rs794727123
1000 genomes	rs794727123
hgdp	rs794727123
ensembl	rs794727123
geneview	rs794727123
scholar	rs794727123
google	rs794727123
pharmgkb	rs794727123
gwascentral	rs794727123
openSNP	rs794727123
23andMe	rs794727123
SNPshot	rs794727123
SNPdbe	rs794727123
MSV3d	rs794727123
GWAS Ctlg	rs794727123

Max Magnitude

0

ClinVar
Risk	rs794727123(A;A)
Alt	rs794727123(A;A)
Reference	Rs794727123(G;G)
Significance	Pathogenic
Disease	Becker muscular dystrophy Duchenne muscular dystrophy
Variation	info
Gene	DMD
CLNDBN	Becker muscular dystrophy Duchenne muscular dystrophy
Reversed	1
HGVS	NC_000023.10:g.32591861C>T
CLNSRC
CLNACC	RCV000174742.1, RCV000174743.1,